dc.creatorConstandil, Luis
dc.creatorHernández, Alejandro
dc.creatorPelissier Serrano, Teresa
dc.creatorArriagada, Osvaldo
dc.creatorEspinoza, Karla
dc.creatorBurgos, Hector
dc.creatorLaurido, Claudio
dc.date.accessioned2019-03-11T12:58:12Z
dc.date.available2019-03-11T12:58:12Z
dc.date.created2019-03-11T12:58:12Z
dc.date.issued2009
dc.identifierArthritis Research and Therapy, Volumen 11, Issue 4, 2018,
dc.identifier14786354
dc.identifier14786362
dc.identifier10.1186/ar2756
dc.identifierhttps://repositorio.uchile.cl/handle/2250/164842
dc.description.abstractIntroduction: Cytokines produced by spinal cord glia after peripheral injuries have a relevant role in the maintenance of pain states. Thus, while IL-1β is overexpressed in the spinal cords of animals submitted to experimental arthritis and other chronic pain models, intrathecal administration of IL-1β to healthy animals induces hyperalgesia and allodynia and enhances wind-up activity in dorsal horn neurons. Methods: To investigate the functional contribution of glial cells in the spinal cord nociceptive transmission, the effect of intrathecally administered IL-1β was studied in both normal and adjuvant-induced arthritic rats with or without glial inhibition. Four weeks after induction of monoarthritis, rats were treated with the glial cell inhibitor propentofylline (10 μg i.t. daily during 10 days) and submitted to a C-fiber-mediated reflex paradigm evoked by single and repetitive (wind-up) electric stimulation. Results: Both the propentofylline treatment and the monoarthritic conditi
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceArthritis Research and Therapy
dc.subjectRheumatology
dc.subjectImmunology
dc.subjectImmunology and Allergy
dc.subjectMedicine (all)
dc.titleEffect of interleukin-1β on spinal cord nociceptive transmission of normal and monoarthritic rats after disruption of glial function
dc.typeArtículos de revistas


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